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在1分钟内于锌阳极上构建超薄固体电解质界面以实现高电流工作条件。

Construction of ultrathin solid electrolyte interface on Zn anode within 1 min for high current operating condition.

作者信息

Liu Jingwen, Ren Junfeng, Li Yongkang, Wang Yuchen, Li Caixia, Wu Zexing, Lai Jianping, Yang Yu, Wang Lei

机构信息

State Key Laboratory Base of Eco-Chemical Engineering, International Science and Technology Cooperation Base of Eco-chemical Engineering and Green Manufacturing, Qingdao University of Science and Technology, Qingdao 266042, China; College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, China.

State Key Laboratory Base of Eco-Chemical Engineering, International Science and Technology Cooperation Base of Eco-chemical Engineering and Green Manufacturing, Qingdao University of Science and Technology, Qingdao 266042, China; Shandong Haihua Co., Ltd., Weifang, Shandong 262737, China.

出版信息

J Colloid Interface Sci. 2024 Nov;673:153-162. doi: 10.1016/j.jcis.2024.06.053. Epub 2024 Jun 7.

Abstract

Organic acid treatment can facilitate the in-situ formation of a solid electrolyte interface (SEI) on Zn foil protecting the anode from corrosion. However, the generation of hydrogen (H) during this process is inevitable, which is often considered detrimental to getting compact SEI. Herein, a H film-assisted method is proposed under concentrated Amino-Trimethylene-Phosphonic-Acid to construct ultrathin and dense SEI within 1 min. Specifically, the (002) crystal planes survive from the etching process of 1 min due to the adhered H, inducing uniform deposition and enhanced corrosion-resistance. Moreover, the H can effectively regulate the reaction rate, leading to ultrathin SEI and initiating a morphology preservation behavior, which has been neglected by the previous reports. The quick-formed SEI has excellent compatibility, low resistance and effective isolation of electrolyte/anode, whose advantages work together with exposed (002) planes to get accustomed to high-current surge, leading to the ZAC1@Zn//ZAC1@Zn consistently cycling over 800 h at 15 mA cm and 15 mAh cm, the ZAC1@Zn//Cu preserves high reversibility (CE 99.7 %), and the ZAC1@Zn//MVO exhibits notable capacity retention at 191.7 mAh/g after 1000 cycles.

摘要

有机酸处理可以促进在锌箔上原位形成固体电解质界面(SEI),保护阳极免受腐蚀。然而,在此过程中氢气(H)的产生是不可避免的,这通常被认为不利于获得致密的SEI。在此,提出了一种在浓氨基三亚甲基膦酸下的氢膜辅助方法,以在1分钟内构建超薄且致密的SEI。具体而言,由于附着的氢,(002)晶面在1分钟的蚀刻过程中得以保留,从而诱导均匀沉积并增强耐腐蚀性。此外,氢可以有效调节反应速率,导致形成超薄SEI并引发形态保留行为,这一点在以前的报道中被忽视了。快速形成的SEI具有优异的兼容性、低电阻以及对电解质/阳极的有效隔离,其优势与暴露的(002)平面共同作用,以适应高电流冲击,使得ZAC1@Zn//ZAC1@Zn在15 mA cm²和15 mAh cm²下持续循环超过800小时,ZAC1@Zn//Cu保持高可逆性(CE 99.7%),并且ZAC1@Zn//MVO在1000次循环后在191.7 mAh/g时表现出显著的容量保持率。

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